Abstract
Both patients and physicians prefer the oral route of drug delivery. The gastrointestinal (GI) tract, though, limits the bioavailability of certain therapeutics because of its protease and bacteria-rich environment as well as general pH variability from pH 1 to 7. These extreme environments make oral delivery particularly challenging for the biologic class of therapeutics. Here, we demonstrate proof-of-concept experiments in swine that microneedle-based delivery has the capacity for improved bioavailability of a biologically active macromolecule. Moreover, we show that microneedle-containing devices can be passed and excreted from the GI tract safely. These findings strongly support the success of implementation of microneedle technology for use in the GI tract.
| Original language | English |
|---|---|
| Pages (from-to) | 362-367 |
| Number of pages | 6 |
| Journal | Journal of Pharmaceutical Sciences |
| Volume | 104 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1 Jan 2015 |
| Externally published | Yes |
Keywords
- Drug delivery systems
- Gastrointestinal
- Macromolecular drug delivery
- Membrane transport
- Microneedles
- Mucosal drug delivery
- Oral drug delivery
- Pill
ASJC Scopus subject areas
- Pharmaceutical Science
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